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单细胞分析揭示了抗菌分子穿孔素-2在人类皮肤中的特定分布,以及其在创伤和金黄色葡萄球菌感染时的调节作用。

Single cell analyses reveal specific distribution of anti-bacterial molecule Perforin-2 in human skin and its modulation by wounding and Staphylococcus aureus infection.

机构信息

Department of Microbiology and Immunology, University of Miami Miller School of Medicine, Miami, Florida.

Department of Dermatology and Cutaneous Surgery, Wound Healing and Regenerative Medicine Research Program, University of Miami Miller School of Medicine, Miami, Florida.

出版信息

Exp Dermatol. 2019 Mar;28(3):225-232. doi: 10.1111/exd.13870. Epub 2019 Feb 12.

Abstract

Perforin-2 (P-2) is a recently described antimicrobial protein with unique properties to kill intracellular bacteria. We investigated P-2 expression pattern and cellular distribution in human skin and its importance in restoration of barrier function during wound healing process and infection with the common wound pathogen Staphylococcus aureus. We describe a novel approach for the measurement of P-2 mRNA within individual skin cells using an amplified fluorescence in situ hybridization (FISH) technique. The unique aspect of this approach is simultaneous detection of P-2 mRNA in combination with immune-phenotyping for cell surface proteins using fluorochrome-conjugated antibodies. We detected P-2 transcript in both hematopoietic (CD45 ) and non-hematopoietic (CD45 ) cutaneous cell populations, confirming the P-2 expression in both professional and non-professional phagocytes. Furthermore, we found an induction of P-2 during wound healing. P-2 overexpression resulted in a reduction of intracellular S. aureus, while infection of human wounds by this pathogen resulted in P-2 suppression, revealing a novel mechanism by which S. aureus may escape cutaneous immunity to cause persistent wound infections.

摘要

穿孔素 2(P-2)是一种最近描述的具有独特特性的抗微生物蛋白,可以杀死细胞内细菌。我们研究了 P-2 在人类皮肤中的表达模式和细胞分布,以及其在伤口愈合过程中和感染常见伤口病原体金黄色葡萄球菌时恢复屏障功能中的重要性。我们描述了一种使用扩增荧光原位杂交(FISH)技术测量单个皮肤细胞内 P-2 mRNA 的新方法。这种方法的独特之处在于,它可以同时检测 P-2 mRNA,并结合使用荧光标记抗体对细胞表面蛋白进行免疫表型分析。我们在造血细胞(CD45)和非造血细胞(CD45)皮肤细胞群中均检测到 P-2 转录本,证实了 P-2 在专业和非专业吞噬细胞中的表达。此外,我们发现 P-2 在伤口愈合过程中被诱导。P-2 的过表达导致细胞内金黄色葡萄球菌减少,而这种病原体感染人体伤口会导致 P-2 抑制,揭示了金黄色葡萄球菌可能逃避皮肤免疫以导致持续伤口感染的新机制。

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